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Frontiers in Oncology
(Aug 2016)
MLH1 Ile219Val polymorphism in Argentinean families with suspected Lynch syndrome
Mev Dominguez-Valentin,
Patrik Wernhoff,
Andrea Romina Cajal,
Pablo German Kalfayan,
Tamara Pinero,
Maria Laura Gonzalez,
Alejandra Ferro,
Ines Sammartino,
Natalia Soledad Causada,
Carlos Alberto Vaccaro
Affiliations
Mev Dominguez-Valentin
Oslo University Hospital
Patrik Wernhoff
Department of Experimental Medical Science, Unit of Muscle Biology, Lund Transgenic Core Facility/Reproductive Immunology
Andrea Romina Cajal
Institute of Basic Sciences and Experimental Medicine (ICBME), Instituto Universitario Hospital Italiano
Pablo German Kalfayan
Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires
Tamara Pinero
Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires
Maria Laura Gonzalez
Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires
Alejandra Ferro
Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires
Ines Sammartino
Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires
Natalia Soledad Causada
Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires
Carlos Alberto Vaccaro
Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires
DOI
https://doi.org/10.3389/fonc.2016.00189
Journal volume & issue
Vol. 6
Abstract
Read online
No abstracts available.
Keywords
Mutation
Lynch Syndrome
MLH1
MSH2
I219V
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